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Gene Gene information from NCBI Gene database.
Entrez ID 55032
Gene name Solute carrier family 35 member A5
Gene symbol SLC35A5
Synonyms (NCBI Gene)
-
Chromosome 3
Chromosome location 3q13.2
Summary This gene encodes a transmembrane protein which belongs to subfamily 35A of the solute carrier superfamily. The encoded protein is a nucleoside-sugar transporter. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2017]
miRNA miRNA information provided by mirtarbase database.
314 Show/Hide all (314)
miRTarBase ID miRNA Experiments Reference
MIRT023910 hsa-miR-1-3p Microarray 18668037
MIRT025853 hsa-miR-7-5p Microarray 19073608
MIRT699358 hsa-miR-335-5p HITS-CLIP 23313552
MIRT699357 hsa-miR-558 HITS-CLIP 23313552
MIRT554213 hsa-miR-3129-3p PAR-CLIP 21572407
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
12 Show/Hide all (12)
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane IBA
GO:0000139 Component Golgi membrane IDA 30641943
GO:0000139 Component Golgi membrane IEA
GO:0005515 Function Protein binding IPI 32296183
GO:0005794 Component Golgi apparatus IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
620298 20792 ENSG00000138459
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9BS91
Protein name UDP-sugar transporter protein SLC35A5 (Solute carrier family 35 member A5)
Protein function Probable UDP-sugar:UMP transmembrane antiporter involved in UDP-alpha-D-glucuronate/UDP-GlcA, UDP-GlcNAc/UDP-N-acetyl-alpha-D-glucosamine and UDP-N-acetyl-alpha-D-galactosamine/UDP-GalNAc transport from the cytosol to the lumen of the Golgi. {EC
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF04142 Nuc_sug_transp 14 → 374 Nucleotide-sugar transporter Family
Sequence
Sequence length 424
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Reference Evidence Score
Monoclonal B-Cell Lymphocytosis Uncertain significance ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Thymoma Uncertain significance ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations